RS876657656 OTOG

Health Risk Chr 11:17574878
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 18B
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 18B
Other Variants in OTOG
rs1029389440 rs397514607 rs397514608 rs183470913 rs191662816 rs545257884 rs552304627 rs876657657 rs61978648 rs191354103
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